Argyrophilic nucleolar organizing regions in patients with Xeroderma Pigmentosum Group E

Autor:	Recep Eröz, Ebru Karagün
Přispěvatelé:	[Belirlenecek]
Rok vydání:	2020
Předmět:	0301 basic medicine medicine.medical_specialty Xeroderma pigmentosum nucleolar organizing regions Skin Neoplasms Adolescent Nose Neoplasms DDB2 rDNA Dermatology Disease Biochemistry Xeroderma Pigmentosum Group E Neoplasms Multiple Primary 030207 dermatology & venereal diseases 03 medical and health sciences 0302 clinical medicine Carcinoma Basosquamous Medicine Abnormal pigmentation Humans In patient skin and connective tissue diseases Molecular Biology Gene Mouth Xeroderma Pigmentosum integumentary system business.industry Eye Neoplasms Genodermatosis Antigens Nuclear Epithelial Cells medicine.disease AgNOR DNA-Binding Proteins 030104 developmental biology Carcinoma Basal Cell Mutation Carcinoma Squamous Cell Sun exposure Skin cancer business
Zdroj:	Experimental dermatologyREFERENCES. 30(3)
ISSN:	1600-0625
Popis:	Xeroderma pigmentosum E (XP-E) is a rare autosomal recessive inherited genodermatosis associated with less severe sun burning with minimal sun exposure. The affected individuals acquire abnormal pigmentation and are at high risk for skin cancer [1] . Notably, the DNA damage-binding protein 2 (DDB2) gene is responsible for XP- E disease [2] .
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76510d91040301bef4d984c6681fe31 https://pubmed.ncbi.nlm.nih.gov/33200418 Zobrazit plný text záznamu Plný text